Skip to content

The Effects of Thrust Joint Manipulation on the Resting and Contracting Thickness of Transversus Abdominis in Subjects With Low Back Pain

The Effects of Thrust Joint Manipulation on the Resting and Contracting Thickness of Transversus Abdominis in Subjects With Low Back Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02558855
Enrollment
67
Registered
2015-09-24
Start date
2015-01-31
Completion date
2015-11-30
Last updated
2016-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

Thrust Joint Manipulation, Non-thrust Joint Manipulation, Transversus Abdominis

Brief summary

The primary aim of this study is to examine how different physical therapy interventions affect the resting state and contraction state of a certain abdominal muscle in patients with low back pain.

Detailed description

Patients with low back pain (LBP) will undergo ultrasound imaging of the transversus abdominis to measure the muscle thickness at rest and at the contracted state prior to intervention and again immediately after intervention. In this randomized controlled trial, patients will be randomized into one of two groups. One group will receive the intervention of thrust joint manipulation of the lumbar spine and the other group will receive the intervention of non-thrust joint manipulation of the lumbar spine.

Interventions

OTHERThrust Joint Manipulation of the Lumbar Spine
OTHERNon-thrust Joint Manipulation of the Lumbar Spine

Sponsors

DeRosa Physical Therapy
CollaboratorUNKNOWN
University of Nevada, Las Vegas
CollaboratorOTHER
Nova Southeastern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Adults between 18-70 years of age with primary symptom of LBP, with or without referral into lower extremity. * Subjects must be able to read and write in English.

Exclusion criteria

* Presence of serious pathology. * Diagnosis of spinal stenosis or symptoms in both lower legs (changes in sensation, muscle weakness). * Any history of low back surgery, rheumatoid arthritis, osteoporosis, osteopenia, scoliosis, or ankylosing spondylitis. * Pregnancy * Pending legal action. * Prior surgery to the lumbar spine or fractures of the lumbar spine.

Design outcomes

Primary

MeasureTime frameDescription
Transversus Abdominis thickness change.Baseline to immediately after the intervention (within 5 minutes).Measurement of change in thickness from resting to contraction will be compared at baseline (pre-intervention) to immediately following the intervention (post-intervention). The study is looking at the immediate effects so there is no short-term or longer follow up.

Secondary

MeasureTime frameDescription
Oswestry Low Back Pain QuestionnaireBaseline, immediately post-intervention (within 5 minutes), and follow-up within 48 hours over the phone.The score of the Oswestry Low Back Pain Questionnaire will be compared from baseline, immediately post-intervention (within 5 minutes), and follow-up within 48 hours over the phone.
Numeric Pain Rating ScaleBaseline, immediately post-intervention (within 5 minutes), and follow-up within 48 hours over the phone.The score of the Numeric Pain Rating Scale will be compared from baseline, immediately post-intervention (within 5 minutes), and follow-up within 48 hours over the phone.
Fear-Avoidance Beliefs QuestionnaireBaseline, immediately post-intervention (within 5 minutes), and follow-up within 48 hours over the phone.The score of the Fear-Avoidance Beliefs Questionnaire will be compared from baseline, immediately post-intervention (within 5 minutes), and follow-up within 48 hours over the phone.
Global Rating of ChangeImmediately post-intervention (within 5 minutes) and at follow-up within 48 hours over the phone.The score of the Global Rating of Change will be compared from immediately post-intervention (within 5 minutes) and follow-up within 48 hours over the phone.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026